Quality & Regulatory Specialist

🕒 April 22

🇬🇧 United Kingdom – Remote

💵 £45k - £55k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🚔 Compliance

👻 Ghost score 64%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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VeroHR

WebsiteLinkedInAll Job Openings

11 - 50 employees

💼 Consulting

🏥 Healthcare

⚖️ Legal

Consulting • Healthcare • Legal

VeroHR is a comprehensive provider of human resource services, technology, and consultancy, offering tailored solutions to transform and enhance organizational operations. It specializes in HR outsourcing, consultancy, payroll services, recruitment support, learning and development, and employment law across diverse sectors including small businesses, startups, charities, and construction. VeroHR is committed to delivering expert guidance in people management strategies, ensuring employee well-being, and fostering leadership development. They operate extensively in the UK, Europe, and internationally, supporting a wide range of clients from startups to large corporate organizations. Their HR services are designed to improve commercial efficiencies, with a strong focus on client success and personalized HR support.

📋 Description

• Deliver quality and regulatory client projects focused on medical devices with software elements • Educate clients on why regulatory documentation is needed, not just what is required • Create, review, and structure medical device technical documentation • Support quality and design activities aligned to medical device regulations and standards • Help clients compile and organise documentation into regulator-ready formats • Adapt internal templates to meet specific client and product needs • Lead and contribute to client meetings, guiding discussions with clarity and confidence • Liaise closely with software engineers, product teams, HR, and senior stakeholders • Work collaboratively with colleagues to deliver joined-up, practical solutions • Manage and deliver multiple client projects simultaneously in a consulting environment

🎯 Requirements

• Background in software-based medical devices • Experience working within medical device quality management environments • Experience working closely with engineers, supporting, guiding, and helping shape documentation alongside development teams • Strong understanding of quality and regulatory expectations for medical devices • Confident communication with stakeholders ranging from highly technical engineers to senior leadership • Highly organised, methodical, and detail-driven • Ability to work independently while contributing to a collaborative team • Medical device technical documentation experience • ISO 13485 or other medical device standards knowledge • Gap analysis or internal auditing experience • Experience reviewing complex technical documentation • Process and procedure development experience • Exposure to AI or advanced software within medical devices • Client-facing consultancy experience

🏖️ Benefits

• 28 days annual leave, including bank holidays plus your birthday off • Fully remote working with quarterly in-person team events (expenses covered) • Vitality Healthcare • Life Assurance (4x salary) • Ongoing professional development and support for further certifications • Progression opportunities • Flexible working designed to support a healthy work-life balance